Department of Chemistry and Biochemistry, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Department of Chemical and Biomolecular Engineering, UCLA, Los Angeles, CA, USA.
Science. 2018 Jan 19;359(6373):343-347. doi: 10.1126/science.aao5167. Epub 2018 Jan 4.
Improving our ability to construct and functionally characterize DNA sequences would broadly accelerate progress in biology. Here, we introduce DropSynth, a scalable, low-cost method to build thousands of defined gene-length constructs in a pooled (multiplexed) manner. DropSynth uses a library of barcoded beads that pull down the oligonucleotides necessary for a gene's assembly, which are then processed and assembled in water-in-oil emulsions. We used DropSynth to successfully build more than 7000 synthetic genes that encode phylogenetically diverse homologs of two essential genes in We tested the ability of phosphopantetheine adenylyltransferase homologs to complement a knockout strain in multiplex, revealing core functional motifs and reasons underlying homolog incompatibility. DropSynth coupled with multiplexed functional assays allows us to rationally explore sequence-function relationships at an unprecedented scale.
提高我们构建和功能表征 DNA 序列的能力将广泛加速生物学的发展。在这里,我们介绍了 DropSynth,这是一种可扩展的、低成本的方法,可以以汇集(多路复用)的方式构建数千个定义的基因长度构建体。DropSynth 使用了一个带有条形码珠子的文库,这些珠子可以下拉基因组装所需的寡核苷酸,然后在油包水乳液中进行处理和组装。我们使用 DropSynth 成功构建了超过 7000 个合成基因,这些基因编码了两种必需基因在系统发育上多样化的同源物。我们在多路复用中测试了磷酸泛酰巯基乙胺腺苷酰转移酶同源物补充敲除 菌株的能力,揭示了核心功能基序和同源物不兼容的原因。DropSynth 与多路复用功能测定相结合,使我们能够以前所未有的规模合理探索序列-功能关系。